Cesare Manetti
Sapienza University of Rome
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Featured researches published by Cesare Manetti.
Nature Communications | 2012
Giovanni Blandino; Mariacristina Valerio; Mario Cioce; Federica Mori; Luca Casadei; Claudio Pulito; Andrea Sacconi; Francesca Biagioni; Giancarlo Cortese; Sergio Galanti; Cesare Manetti; Gennaro Citro; Paola Muti; Sabrina Strano
Diabetic patients treated with metformin have a reduced incidence of cancer and cancer-related mortality. Here we show that metformin affects engraftment and growth of breast cancer tumours in mice. This correlates with the induction of metabolic changes compatible with clear anticancer effects. We demonstrate that microRNA modulation underlies the anticancer metabolic actions of metformin. In fact, metformin induces DICER expression and its effects are severely impaired in DICER knocked down cells. Conversely, ectopic expression of DICER recapitulates the effects of metformin in vivo and in vitro. The microRNAs upregulated by metformin belong mainly to energy metabolism pathways. Among the messenger RNAs downregulated by metformin, we found c-MYC, IRS-2 and HIF1alpha. Downregulation of c-MYC requires AMP-activated protein kinase-signalling and mir33a upregulation by metformin. Ectopic expression of c-MYC attenuates the anticancer metabolic effects of metformin. We suggest that DICER modulation, mir33a upregulation and c-MYC targeting have an important role in the anticancer metabolic effects of metformin.
Physical Review E | 1999
Cesare Manetti; Marc-Antoine Ceruso; Charles L. Webber; Joseph P. Zbilut
A molecular dynamics simulation of a Lennard-Jones fluid and a trajectory of the B1 immunoglobulin G-binding domain of streptococcal protein G (B1-IgG) simulated in water are analyzed by recurrence quantification, which is noteworthy for its independence from stationarity constraints, as well as its ability to detect transients and both linear and nonlinear state changes. The results demonstrate the sensitivity of the technique for the discrimination of phase sensitive dynamics. The physical interpretation of the recurrence measures is also discussed.
Biophysical Journal | 2003
Joseph P. Zbilut; Alfredo Colosimo; Filippo Conti; Mauro Colafranceschi; Cesare Manetti; Mariacristina Valerio; Charles L. Webber
The problem of protein folding vs. aggregation was investigated in acylphosphatase and the amyloid protein Abeta(1-40) by means of nonlinear signal analysis of their chain hydrophobicity. Numerical descriptors of recurrence patterns provided the basis for statistical evaluation of folding/aggregation distinctive features. Static and dynamic approaches were used to elucidate conditions coincident with folding vs. aggregation using comparisons with known protein secondary structure classifications, site-directed mutagenesis studies of acylphosphatase, and molecular dynamics simulations of amyloid protein, Abeta(1-40). The results suggest that a feature derived from principal component space characterized by the smoothness of singular, deterministic hydrophobicity patches plays a significant role in the conditions governing protein aggregation.
Proteins | 2004
Mariacristina Valerio; Alfredo Colosimo; Filippo Conti; Alessandro Grottesi; Cesare Manetti; Joseph P. Zbilut
In a previous article (Zbilut et al., Biophys J 2003;85:3544–3557), we demonstrated how an aggregation versus folding choice could be approached considering hydrophobicity distribution and charge. In this work, our aim is highlighting the mutual interaction of charge and hydrophobicity distribution in the aggregation process. Use was made of two different peptides, both derived from a transmembrane protein (amyloid precursor protein; APP), namely, Aβ(1‐28) and Aβ(1‐40). Aβ(1‐28) has a much lower aggregation propensity than Aβ(1‐40). The results obtained by means of molecular dynamics simulations show that, when submitted to the most “aggregation‐prone” environment, corresponding to the isoelectric point and consequently to zero net charge, both peptides acquire their maximum flexibility, but Aβ(1‐40) has a definitely higher conformational mobility than Aβ(1‐28). The absence of a hydrophobic “tail,” which is the most mobile part of the molecule in Aβ(1‐40), is the element lacking in Aβ(1‐28) for obtaining a “fully aggregating” phenotype. Our results suggest that conformational flexibility, determined by both hydrophobicity and charge effect, is the main mechanistic determinant of aggregation propensity. Proteins 2005.
RSC Advances | 2014
Francesca Costantini; A. Nascetti; R. Scipinotti; Fabio Domenici; Simona Sennato; Laura Gazza; F. Bordi; Norberto Pogna; Cesare Manetti; D. Caputo; Giampiero de Cesare
In this paper, we present the preliminary results of an ELISA-on-chip device, intended as a technological demonstrator of a novel analytical system suitable for the diagnosis and follow-up of celiac disease. The idea of the work is to combine an array of amorphous silicon photosensors with a pattern of a poly(2-hydroxyethyl methacrylate) polymer brush film, which acts as anchor for the immobilization of gliadin peptides containing the celiac disease epitopes. Recognition relies on a sandwich immunoassay between antibodies against the peptides and secondary antibodies marked with horseradish peroxidase to obtain a chemiluminescent signal. Detection is based on the measurement of photocurrent induced in the array of amorphous silicon photosensors by the chemiluminescent signal. An ad-hoc procedure has been developed in order to enable the fabrication of the photodiode array and the polymer brush pattern on the two sides of the same glass substrate ensuring the compatibility of the different technological steps. The sensitivity and the selectivity of the chip for multiplex immunoassays were demonstrated using two gliadin peptides (VEA and DEC). In particular, we found that the average amount of the bound HRP revealed by our analytical protocol is 3.5(±0.3) × 10−6 pg μm−2 and 0.85(±0.3) × 10−6 pg μm−2 for specific and non-specific interactions, respectively.
Neurochemical Research | 2000
Tommaso Aureli; Maria Enrica Di Cocco; G. Capuani; Rita Ricciolini; Cesare Manetti; Alfredo Miccheli; Filippo Conti
Changes in brain lipid composition have been determined in 24 months-old Fischer rats with respect to 6 months-old ones. The cerebral levels of sphingomyelin and cholesterol were found to be significantly increased in aged rats, whereas the amount of phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, phosphatidylinositol, and phosphatidic acid appear to be unaffected by aging. Long-term feeding with acetyl-L-carnitine was able to reduce the age-dependent increase of both sphingomyelin and cholesterol cerebral levels with no effect on the other measured phospholipids. These findings shown that changes in membrane lipid metabolism and/or composition represent one of the alterations occurring in rat brain with aging, and that long-term feeding with acetyl-L-carnitine can be useful in normalizing these age-dependent disturbances.
Cell Biochemistry and Biophysics | 2002
Joseph P. Zbilut; Paolo Sirabella; Cesare Manetti; Alfredo Colosimo; Charles L. Webber
This review considers the use of a nonlinear signal analysis tool, recurrence quantification analysis, as a method to study sequence/structure relationships of proteins. Four broad categories are discussed: (1) a point of view involving information contained in deterministic aspects of hydrophobicity; (2) the analysis of protein hydrophobicity “singularities”; (3) time-series analysis of protein dynamics simulations; and (4) prediction of protein secondary structure.
Current Allergy and Asthma Reports | 2014
Rossana Scrivo; Luca Casadei; Mariacristina Valerio; Roberta Priori; Guido Valesini; Cesare Manetti
Metabolomics is the analysis of the concentration profiles of low molecular weight compounds present in biological fluids. Metabolites are nonpeptide molecules representing the end products of cellular activity. Therefore, changes in metabolite concentrations reveal the range of biochemical effects induced by a disease or its therapeutic intervention. Metabolomics has recently become feasible with the accessibility of new technologies, including mass spectrometry and high-resolution proton nuclear magnetic resonance, and has already been applied to several disorders. Indeed, it has the advantage of being a nontargeted approach for identifying potential biomarkers, which means that it does not require a preliminary knowledge of the substances to be studied. In this review, we summarize the main studies in which metabolomic approach was used in some allergic (asthma, atopic dermatitis) and rheumatic diseases (rheumatoid arthritis, systemic lupus erythematosus) to explore the feasibility of this technique as a novel diagnostic tool in these complex disorders.
Brain Research | 1998
Tommaso Aureli; Maria Enrica Di Cocco; Caterina Puccetti; Rita Ricciolini; Maurizio Scalibastri; Alfredo Miccheli; Cesare Manetti; Filippo Conti
The effects of acetyl-L-carnitine on cerebral glucose metabolism were investigated in rats injected with differently 14C- and 13C-labelled glucose and sacrificed after 15, 30, 45, and 60 min. Acetyl-L-carnitine was found to reduce total 14CO2 release from [U-14C]glucose along with the decrease in [1-13C]glucose incorporation into cerebral amino acids and tricarboxylic acid cycle intermediates. However the 13C labelling pattern within different carbon positions of glutamate, glutamine, GABA, and aspartate was unaffected by acetyl-L-carnitine administration. Furthermore, the cerebral levels of newly-synthesized proglycogen were higher in rats treated with acetyl-L-carnitine than in untreated ones. These results suggest that acetyl-L-carnitine was able to modulate cerebral glucose utilization and provide new insights on the mechanisms of action of this molecule in the central nervous system.
Polymer | 2002
Cesare Manetti; Lorena Casciani; Nicola Pescosolido
The biocompatibility of contact lenses is closely related to their oxygen permeability. In hydrogel lenses, this characteristic can be attributed to the water permeability resulting from a combination of viscous and diffusive fluxes. Hydrogel lenses were studied by means of nuclear magnetic resonance (NMR) relaxation times, resulting in a mathematical model which evaluated the water self-diffusion coefficient as a quantification of the diffusive contribution to permeation. Comparing the results obtained with the data of permeability to oxygen as measured by other techniques, a reasonable agreement was shown for lenses with a higher water content (WC) with respect to lenses with a lower WC: this difference was accounted for by considering the different contribution to permeation.